As so many across the rare disease community can attest to, the journey to finding a correct diagnosis for a rare disease is a lengthy, emotional process. At times, even after receiving a diagnosis, families can still feel lost. We felt that way after Yash's diagnosis, and that is what led to the creation of the Yash Gandhi Foundation.
We are proud to announce that we have created a new Diagnosis Handbook to help guide families on their Mucolipidosis journey. The Handbook is available by clicking the cover image below.
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